Highly chemoselective reductive amination by one pot reaction of aldehydes, amines and Dihydropyridine Catalyzed by TMSCl-Reference-Cited by-同舟云学术

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Highly chemoselective reductive amination by one pot reaction of aldehydes, amines and Dihydropyridine Catalyzed by TMSCl

Published:2010-06 Issue:2 Volume:7 Page:428-431
ISSN:1735-207X
Container-title:Journal of the Iranian Chemical Society
language:en
Short-container-title:JICS

Author:

Azizi N.,Khajeh Amiri A. R.,Ghafuri H.,Saidi M. R.,Bolourtchian M.

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/BF03246028.pdf

Reference39 articles.

1. S.J. Connon, Org. Biomol. Chem. (2007) 3407.

2. T. Henkel, R.M. Brunne, H. Mueller, F. Reichel, Angew. Chem. Int. Ed. 38 (1999) 643.

3. K.W. Henderson, W.J. Kerr, J.H. Moir, Chem. Commun. (2000) 479.

4. V. Gotor-Fernandez, P. Fernandez-Torres, V. Gotor, Tetrahedron Asy. 17 (2006) 2558.

5. M.F.A. Adamo, V.K. Aggarwal, M.A. Sage, J. Am. Chem. Soc. 122 (2000) 8317.

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5. Chlorotrimethylsilane (TMSCl): an efficient silicon-based Lewis acid mediator in allylic alkylation using a diethylzinc reagent;RSC Adv.;2014

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